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Main Authors: Amandine L. Flourat, Damien Breilly, Floriane Rischard, Aurélien A. M. Péru, Rémi Estorges, Abdouramane Dosso, Sami Fadlallah, Antoine Gallos, Florent Allais
Format: Artículo Open Access
Published: Wiley 2026
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Online Access:https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.70675
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author Amandine L. Flourat
Damien Breilly
Floriane Rischard
Aurélien A. M. Péru
Rémi Estorges
Abdouramane Dosso
Sami Fadlallah
Antoine Gallos
Florent Allais
author_facet Amandine L. Flourat
Damien Breilly
Floriane Rischard
Aurélien A. M. Péru
Rémi Estorges
Abdouramane Dosso
Sami Fadlallah
Antoine Gallos
Florent Allais
Amandine L. Flourat
Damien Breilly
Floriane Rischard
Aurélien A. M. Péru
Rémi Estorges
Abdouramane Dosso
Sami Fadlallah
Antoine Gallos
Florent Allais
collection Wiley Open Access
contents Sustainable Syntheses of p ‐Hydroxycinnamic‐Based Macrobisphenols: Progress, Challenges, and Comparative Assessment of Yield and Sustainability Amandine L. Flourat Damien Breilly Floriane Rischard Aurélien A. M. Péru Rémi Estorges Abdouramane Dosso Sami Fadlallah Antoine Gallos Florent Allais ChemSusChem Macrobisphenols are a family of bio‐inspired bisphenols introduced in 2013, composed of two p ‐hydroxycinnamate units linked through ester bonds via a polyol scaffold. Unlike bisphenol A, macrobisphenols are non‐endocrine‐disrupting compounds, and display outstanding antiradical activity, making them attractive, safer alternatives for polymer‐related applications. Their versatility enables use as plasticizers, antioxidants, and monomers for polymer and materials synthesis. Over the past 12 years, substantial progress has been made to enhance their industrial viability by expanding structural diversity through extensive libraries of analogs, significantly lowering production costs, and minimizing environmental impact through greener synthetic strategies. This article critically reviews the evolution of macrobisphenol synthesis, highlights recent advances in sustainable and scalable pathways, and provides practical guidelines for selecting the most cost‐effective and environmentally responsible processes according to the targeted structure. 10.1002/cssc.70675 http://creativecommons.org/licenses/by-nc-nd/4.0/
doi_str_mv 10.1002/cssc.70675
format Artículo Open Access
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institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
publishDate 2026
publisher Wiley
record_format wiley_oa
spellingShingle Sustainable Syntheses of p ‐Hydroxycinnamic‐Based Macrobisphenols: Progress, Challenges, and Comparative Assessment of Yield and Sustainability
Amandine L. Flourat
Damien Breilly
Floriane Rischard
Aurélien A. M. Péru
Rémi Estorges
Abdouramane Dosso
Sami Fadlallah
Antoine Gallos
Florent Allais
ChemSusChem
Sustainable Syntheses of p ‐Hydroxycinnamic‐Based Macrobisphenols: Progress, Challenges, and Comparative Assessment of Yield and Sustainability Amandine L. Flourat Damien Breilly Floriane Rischard Aurélien A. M. Péru Rémi Estorges Abdouramane Dosso Sami Fadlallah Antoine Gallos Florent Allais ChemSusChem Macrobisphenols are a family of bio‐inspired bisphenols introduced in 2013, composed of two p ‐hydroxycinnamate units linked through ester bonds via a polyol scaffold. Unlike bisphenol A, macrobisphenols are non‐endocrine‐disrupting compounds, and display outstanding antiradical activity, making them attractive, safer alternatives for polymer‐related applications. Their versatility enables use as plasticizers, antioxidants, and monomers for polymer and materials synthesis. Over the past 12 years, substantial progress has been made to enhance their industrial viability by expanding structural diversity through extensive libraries of analogs, significantly lowering production costs, and minimizing environmental impact through greener synthetic strategies. This article critically reviews the evolution of macrobisphenol synthesis, highlights recent advances in sustainable and scalable pathways, and provides practical guidelines for selecting the most cost‐effective and environmentally responsible processes according to the targeted structure. 10.1002/cssc.70675 http://creativecommons.org/licenses/by-nc-nd/4.0/
title Sustainable Syntheses of p ‐Hydroxycinnamic‐Based Macrobisphenols: Progress, Challenges, and Comparative Assessment of Yield and Sustainability
topic ChemSusChem
url https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.70675